EP1827105A2 - Composition herbicide - Google Patents

Composition herbicide

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Publication number
EP1827105A2
EP1827105A2 EP05824391A EP05824391A EP1827105A2 EP 1827105 A2 EP1827105 A2 EP 1827105A2 EP 05824391 A EP05824391 A EP 05824391A EP 05824391 A EP05824391 A EP 05824391A EP 1827105 A2 EP1827105 A2 EP 1827105A2
Authority
EP
European Patent Office
Prior art keywords
prosulfocarb
metolachlor
composition
crops
mefenacet
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Granted
Application number
EP05824391A
Other languages
German (de)
English (en)
Other versions
EP1827105B1 (fr
Inventor
Georg R. Kotzian
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Syngenta Participations AG
Original Assignee
Syngenta Participations AG
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Syngenta Participations AG filed Critical Syngenta Participations AG
Priority to EP05824391A priority Critical patent/EP1827105B1/fr
Priority to PL05824391T priority patent/PL1827105T3/pl
Priority to EP08022183A priority patent/EP2039249A3/fr
Publication of EP1827105A2 publication Critical patent/EP1827105A2/fr
Application granted granted Critical
Publication of EP1827105B1 publication Critical patent/EP1827105B1/fr
Active legal-status Critical Current
Anticipated expiration legal-status Critical

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Classifications

    • A—HUMAN NECESSITIES
    • A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
    • A01N47/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid
    • A01N47/08—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid the carbon atom having one or more single bonds to nitrogen atoms
    • A01N47/10—Carbamic acid derivatives, i.e. containing the group —O—CO—N<; Thio analogues thereof
    • A01N47/12—Carbamic acid derivatives, i.e. containing the group —O—CO—N<; Thio analogues thereof containing a —O—CO—N< group, or a thio analogue thereof, neither directly attached to a ring nor the nitrogen atom being a member of a heterocyclic ring

Definitions

  • the present invention relates to a herbicidal composition
  • a herbicidal composition comprising a herbicidal active ingredient combination that is preferably suitable for the selective control of undesired vegetation like weeds (grasses and broad-leaved weeds) in crops of useful plants and in particular resistant weeds in crops of useful plants, for example in crops of rice, cereals and maize.
  • the invention relates also to a method of controlling weeds, which are defined as undesired vegetation in crops of useful plants and to the use of the novel composition to act where control is desired, for example, on the undesired vegetation or the locus thereof.
  • the present invention provides the use of the novel composition for control of undesired vegetation, which comprises applying (i) before emergence (pre-emergence) of the undesired vegetation, (ii) after emergence (post-emergence) of the undesired vegetation, or (iii) both (i) and (ii), the composition, in a herbicidally effective amount, where control is desired, for example, on the undesired vegetation or the locus thereof.
  • the compounds prosulfocarb (683), Group K3 / Inhibitors of cell division Inhibitors of VLCFAs (inhib of PDS) naproanilide (571), pretilachlor (656), napropamide (572), diphenamid (274), butachlor (100), acetochlor (5), dimethenamid (260), dimethachlor (258), alachlor (14), metolachlor (548), S-metolachlor (549), propisochlor (677), pethoxamid (627), metazachlor (524), thenylchlor (789), propachlor (667), Group K3 (tetrazolinone), fentrazamide (348), Group K3 (oxyacetamids) flufenacet (369), mefenacet (505), Group K3 (others) anilofos (31), piperophos (650) and cafenstrole (110) and agronomically acceptable salts thereof, exhibit herbicidal action, as
  • variable amounts of prosulfocarb with at least one inhibitor of cell division exhibits a synergistic action that is capable of controlling, both pre-emergence and post-emergence, the majority of weeds (grasses and broad-leaved weeds) occurring especially in crops of useful plants, without appreciably damaging the useful plants, in particular ALS-resistant weeds and ACCase-resistant weeds in crops of useful plants, for example in crops of rice, cereals or maize.
  • a novel herbicidal composition for the selective control of weeds which comprises a) prosulfocarb and b) at least one compound selected from the compounds of the group naproanilide, napropamide, diphenamid, butachlor, acetochlor, dimethenamid, dimethachlor, alachlor, metolachlor, S-metolachlor, propisochlor, pethoxamid, metazachlor, thenylchlor, propachlor, fentrazamide, flufenacet, mefenacet, anilofos, piperophos and cafenstrole.
  • a second aspect of the present invention provides method a of controlling undesired vegetation in crops of useful plants, which comprises allowing a herbicidally effective amount of the composition defined in the first aspect to act where control is desired
  • a method of controlling one or more resistant weeds selected from ALS-resistant weeds, ACCase-resistant weeds, propanil- resistant weeds, and quinclorac-resistant weeds, in crops of useful plants which comprises allowing a herbicidally effective amount of a composition to act where control is desired, wherein the herbicidal composition comprises:
  • prosulfocarb and (b) at least one compound selected from the compounds of the group pretilachlor, naproanilide, napropamide, diphenamid, butachlor, acetochlor, dimethenamid, dimethachlor, alachlor, metolachlor, S-metolachlor, propisochlor, pethoxamid, metazachlor, thenylchlor, propachlor, fentrazamide, flufenacet, mefenacet, anilofos, piperophos and cafenstrole.
  • the herbicidal composition consists essentially of, more preferably consists of, as active ingredient, (a) and (b) as defined herein, and optionally one or more formulation adjuvants.
  • one or more further herbicidal active ingredients are present in the herbicidal composition in combination with (a) and (b).
  • Combinations that are especially effective are: prosulfocarb + naproanilide, prosulfocarb + napropamide, prosulfocarb + diphenamid, prosulfocarb + butachlor, prosulfocarb + acetochlor, prosulfocarb + dimethenamid, prosulfocarb + dimethachlor, prosulfocarb + alachlor, prosulfocarb + metolachlor, prosulfocarb + S-metolachlor, prosulfocarb + propisochlor, prosulfocarb + pethoxamid, prosulfocarb + metazachlor, prosulfocarb + thenylchlor, prosulfocarb + propachlor, prosulfocarb + fentrazamide, prosulfocarb + flufenacet, prosulfocarb + mefenacet, prosulfocarb + anilofos, prosulfo
  • Combinations that have been found to be very especially effective are prosulfocarb + S- metolachlor; prosulfocarb and fentrazamide; prosulfocarb and mefenacet; and prosulfocarb and cafenstrole.
  • composition according to the invention comprises the mentioned active ingredients in any mixing ratio, but usually has an excess of one component over the other.
  • Preferred mixing ratios of the active ingredients are from 25:1 to 1 :25.
  • the rate of application may also vary within wide limits and depends upon the nature of the soil, the method of application (pre- or post-emergence; seed dressing; application to the seed furrow; no tillage application etc.), the crop plant, the weed or grass to be controlled, the prevailing climatic conditions, and other factors governed by the method of application, the specific active ingredient combination, the time of application and the target crop.
  • the active ingredient mixture according to the invention can generally be applied at a rate of 0.05 to 7 kg of active ingredient mixture per hectare, preferably at a rate of 1 to 5 kg of active ingredient mixture per hectare.
  • the invention relates also to a method for the selective control of grasses and weeds in crops of useful plants, which comprises treating the useful plants or the area under cultivation or the locus thereof simultaneously or at different times with the compositions according to the invention.
  • Crops of useful plants in which the composition according to the invention can be used include especially rice.
  • the term "crops" is to be understood as also including crops that have been rendered tolerant to herbicides or classes of herbicides (for example ALS, GS, EPSPS, PPO and HPPD inhibitors) as a result of conventional methods of breeding or genetic engineering.
  • herbicides or classes of herbicides for example ALS, GS, EPSPS, PPO and HPPD inhibitors
  • An example of a crop that has been rendered tolerant e.g. to imid- azolinones, such as imazamox, by conventional methods of breeding is Clearfield® summer rape (Canola).
  • crops that have been rendered tolerant to herbicides by genetic engineering methods include e.g.
  • the weeds to be controlled may be both monocotyledonous and dicotyledonous weeds, such as, for example, Alisma spp, Leptochloa chinensis, Stellaria, Nasturtium, Agrostis, Digitaria, Avena, Setaria, Sinapis, Lolium, Solanum, Echinochloa and especially Echinochloa crus- galli or Echinochloa oryzicola, Scirpus and especially Scirpus juncoides, Monochoria and especially Monochoria vaginalis, Sagittaria and especially Sagittaria pygmea, Bromus, Alopecurus, Sorghum, Rottboellia, Cyperus and especially Cyperus iria, Abutilon, Sida, Xanthium, Amaranthus, Chenopodium
  • Crops are also to be understood as being those which have been rendered resistant to harmful insects by genetic engineering methods, for example Bt maize (resistant to European corn borer), Bt cotton (resistant to cotton boll weevil) and also Bt potatoes (resistant to Colorado beetle).
  • Bt maize are the BM 76 maize hybrids of NK® (Syngenta Seeds).
  • the Bt toxin is a protein that is formed naturally by Bacillus thuringiensis soil bacteria. Examples of toxins and transgenic plants able to synthesise such toxins are described in EP-A-451 878, EP-A-374 753, WO 93/07278, WO 95/34656, WO 03/052073 and EP-A-427 529.
  • transgenic plants that contain one or more genes which code for an insecticidal resistance and express one or more toxins are KnockOut® (maize), Yield Gard® (maize), NuCOTI N33B® (cotton), Bollgard® (cotton), NewLeaf® (potatoes), NatureGard® and Protexcta®.
  • Plant crops and their seed material can be resistant to herbicides and at the same time also to insect feeding ("stacked" transgenic events). Seed can, for example, have the ability to express an insecticidally active Cry3 protein and at the same time be glyphosate-tolerant.
  • the term "crops" is to be understood as also including crops obtained as a result of conventional methods of breeding or genetic engineering which contain so-called output traits (e.g. improved flavour, storage stability, nutritional content).
  • Areas under cultivation are to be understood as including land where the crop plants are already growing as well as land intended for the cultivation of those crop plants.
  • compositions according to the invention can be used in unmodified form.
  • the compositions according to the invention are, however, generally formulated in a variety of way using formulation adjuvants, such as carriers, solvents and surface-active substances.
  • the formulations can be in various physical forms, for example in the form of dusting powders, gels, wettable powders, water-dispersible granules, water-dispersible tablets, effervescent compressed tablets, emulsifiable concentrates, microemulsifiable concentrates, oil-in-water emulsions, oil flowables, aqueous dispersions, oily dispersions, suspoemulsions, capsule suspensions, emulsifiable granules, soluble liquids, water-soluble concentrates (with water or a water-miscible organic solvent as carrier), impregnated polymer films or in other forms known, for example, from the Manual on Development and Use of FAO Specifications for Plant Protection Products, 5th Edition, 1999.
  • the formulations can be prepared, for example, by mixing the active ingredients with formulation adjuvants in order to obtain compositions in the form of finely divided solids, granules, solutions, dispersions or emulsions.
  • the active ingredients can also be formulated with other adjuvants, for example finely divided solids, mineral oils, vegetable oils, modified vegetable oils, organic solvents, water, surface-active substances or combinations thereof.
  • the active ingredients can also be contained in very fine microcapsules consisting of a polymer. Microcapsules contain the active ingredients in a porous carrier. This enables the active ingredients to be released into their surroundings in controlled amounts (e.g. slow release). Microcapsules usually have a diameter of from 0.1 to 500 microns.
  • the active ingredients contain active ingredients in an amount of about from 25 to 95 % by weight of the capsule weight.
  • the active ingredients can be present in the form of a monolithic solid, in the form of fine particles in solid or liquid dispersion or in the form of a suitable solution.
  • the encapsulating membranes comprise, for example, natural and synthetic gums, cellulose, styrene-butadiene copolymers, polyacrylonitrile, polyacrylate, polyester, polyamides, polyureas, polyurethane or chemically modified polymers and starch xanthates or other polymers that are known to the person skilled in the art in this connection.
  • the formulation adjuvants suitable for the preparation of the compositions according to the invention are known perse.
  • liquid carriers there may be used: water, toluene, xylene, petroleum ether, vegetable oils, acetone, methyl ethyl ketone, cyclohexanone, acid anhydrides, acetonitrile, acetophenone, amyl acetate, 2-butanone, butylne carbonate, chlorobenzene, cyclohexane, cyclohexanol, alkyl esters of acetic acid, diacetone alcohol, 1 ,2-dichloropropane, diethanolamine, p-diethylbenzene, diethylene glycol, diethylene glycol abietate, diethylene glycol butyl ether, diethylene glycol ethyl ether, diethylene glycol methyl ether, N,N-dimethylformamide, dimethyl sulfoxide, 1 ,4-dioxane
  • Water is generally the carrier of choice for the dilution of the concentrates.
  • Suitable solid carriers are, for example, talc, titanium dioxide, pyrophyllite clay, silica, attapulgite clay, kieselguhr, limestone, calcium carbonate, bentonite, calcium montomorillonite, cottonseed husks, wheatmeal, soybean flour, pumice, wood flour, ground walnut shells, lignin and similar materials, as described, for example, in CFR 180.1001 . (c) & (d).
  • a large number of surface-active substances can advantageously be used both in solid and in liquid formulations, especially in those formulations which can be diluted with a carrier prior to use.
  • Surface-active substances may be anionic, cationic, non-ionic or polymeric and they may be used as emulsifiying, wetting or suspending agents or for other purposes.
  • Typical surface-active substances include, for example, salts of alkyl sulfates, such as diethanolammonium lauryl sulfate; salts of alkylarylsulfonates, such as calcium dodecyl- benzenesulfonate; alkylphenol-alkylene oxide addition products, such as nonylphenol ethoxylate; alcohol-alkylene oxide addition products, such as tridecyl alcohol ethoxylate; soaps, such as sodium stearate; salts of alkylnaphthalenesulfonat.es, such as sodium dibutylnaphthalenesulfonate; dialkyl esters of sulfosuccinate salts, such as sodium di(2- ethylhexyl)sulfosuccinate
  • Further adjuvants which can usually be used in pesticidal formulations include crystallisation inhibitors, viscosity-modifying substances, suspending agents, dyes, anti-oxidants, foaming agents, light absorbers, mixing aids, anti-foams, complexing agents, neutralising or pH- modifying substances and buffers, corrosion-inhibitors, fragrances, wetting agents, absorption improvers, micronutrients, plasticisers, glidants, lubricants, dispersants, thickeners, anti-freezes, microbiocides and also liquid and solid fertilisers.
  • the formulations may also comprise additional active substances, for example further herbicides, herbicide safeners, plant growth regulators, fungicides or insecticides.
  • compositions according to the invention can additionally include an additive comprising an oil of vegetable or animal origin, a mineral oil, alkyl esters of such oils or mixtures of such ' oils and oil derivatives.
  • the amount of oil additive used in the composition according to the invention is generally from 0.01 to 10 %, based on the spray mixture.
  • the oil additive can be added to the spray tank in the desired concentration after the spray mixture has been prepared.
  • Preferred oil additives comprise mineral oils or an oil of vegetable origin, for example rapeseed oil, olive oil or sunflower oil, emulsified vegetable oil, such as AMIGO® (Rh ⁇ ne-Poulenc Canada Inc.), alkyl esters of oils of vegetable origin, for example the methyl derivatives, or an oil of animal origin, such as fish oil or beef tallow.
  • a preferred additive contains, for example, as active components essentially 80 % by weight alkyl esters of fish oils and 15 % by weight methylated rapeseed oil, and also 5 % by weight of customary emulsifiers and pH modifiers.
  • Especially preferred oil additives comprise alkyl esters of C 8 -C 22 fatty acids, especially the methyl derivatives of Ci 2 -C 18 fatty acids, for example, the methyl esters of lauric acid, palmitic acid and oleic acid, being important; those esters are known as methyl laurate (CAS-111-82-0), methyl palmitate (CAS-112-39-0) and methyl oleate (CAS-112-62-9) respectively.
  • a preferred fatty acid methyl ester derivative is Emery® 2230 or 2231 (Cognis GmbH).
  • Those and other oil derivatives are also known from the Compendium of Herbicide Adjuvants, 5th Edition, Southern Illinois University, 2000.
  • the application and action of the oil additives can be further improved by combining them with surface-active substances, such as non-ionic, anionic or cationic surfactants.
  • surface-active substances such as non-ionic, anionic or cationic surfactants.
  • suitable anionic, non-ionic and cationic surfactants are listed on pages 7 and 8 of WO 97/34485.
  • Preferred surface-active substances are anionic surfactants of the dodecyl- benzylsulfonate type, especially the calcium salts thereof, and also non-ionic surfactants of the fatty alcohol ethoxylate type. Special preference is given to ethoxylated C 12 -C 22 fatty alcohols having a degree of ethoxylation of from 5 to 40.
  • Examples of commercially available surfactants are the Genapol types (Clariant AG).
  • silicone surfactants especially polyalkyl-oxide-modified heptamethyltrisiloxanes, which are commercially available e.g. as Silwet L-77®, and also perfluorinated surfactants.
  • concentration of surface-active substances in relation to the total additive is generally from 1 to 30 % by weight.
  • oil additives that consist of mixtures of oils or mineral oils or derivatives thereof with surfactants are Edenor ME SU®, Turbocharge® (Syngenta AG, CH) and Actipron® (BP Oil UK Limited, GB).
  • the said surface-active substances may also be used in the formulations alone, that is to say without oil additives.
  • an organic solvent to the oil additive/surfactant mixture can contribute to a further enhancement of action.
  • Suitable solvents are, for example,
  • Solvesso® (ESSO) and Aromatic Solvent® (Exxon Corporation).
  • concentration of such solvents can be from 10 to 80 % by weight of the total weight.
  • oil additives which may be in admixture with solvents, are described, for example, in US-A-4 834 908.
  • a commercially available oil additive disclosed therein is known by the name MERGE® (BASF Corporation).
  • a further oil additive that is preferred according to the invention is SCORE® (Syngenta Crop Protection Canada).
  • formulations of alkylpyrrolidones (e.g. Agrimax®) to be added to the spray mixture.
  • Formulations of synthetic latices such as, for example, polyacrylamide, polyvinyl compounds or poly-1-p-menthene (e.g. Bond®, Courier® or Emerald®) can also be used. Solutions that contain propionic acid, for example Eurogkem Pen-e-trate®, can also be mixed into the spray mixture as activity-enhancing agents.
  • the herbicidal formulations generally contain from 0.1 to 99 % by weight, especially from 0.1 to 95 % by weight, of an active ingredient mixture of the compositions according to the invention and from 1 to 99.9 % by weight of a formulation adjuvant, which preferably includes from 0 to 25 % by weight of a surface-active substance.
  • a formulation adjuvant which preferably includes from 0 to 25 % by weight of a surface-active substance.
  • Emulsifiable concentrates active ingredient mixture: 1 to 95 %, preferably 60 to 90 % surface-active agent: 1 to 30 %, preferably 5 to 20 % liquid carrier: balance
  • Dusts active ingredient mixture: 0.1 to 10 %, preferably 0.1 to 5 % solid carrier: 99.9 to 90 %, preferably 99.9 to 99 %
  • Suspension concentrates active ingredient mixture: 5 to 75 %, preferably 10 to 50 % surface-active agent: 1 to 40 %, preferably 2 to 30 % water: balance
  • Wettable powders active ingredient mixture: 0.5 to 90 %, preferably 1 to 80 % surface-active agent: 0.5 to 20 %, preferably 1 to 15 % solid carrier: balance
  • Granules active ingredient mixture: 0.1 to 30 %, preferably 0.5 to 15 % solid carrier: 99.9 to 70 %, preferably 99,5 to 85 %
  • Emulsifiable concentrates a) b) c) d) active ingredient mixture 5% 10% 25 % 50% calcium dodecylbenzene- sulfonate 6% 8% 6 % 8% castor oil polyglycol ether 4% 4 % 4%
  • Emulsions of any desired concentration can be prepared from such concentrates by dilution with water.
  • the solutions are suitable for application in the form of microdrops.
  • Wettable powders a) b) c) d) active ingredient mixture 5% 25% 50 % 80% sodium lignosulfonate 4% - 3' % - sodium lauryl sulfate 2% 3% - 4% sodium diisobutylnaphthalene- sulfonate - 6% 5' % 6% octylphenol polyglycol ether - 1 % 2' % -
  • the finely ground active ingredient is applied uniformly, in a mixer, to the carrier moistened with polyethylene glycol. Non-dusty coated granules are obtained in this manner.
  • Ready-to-use dusts are obtained by mixing the active ingredient with the carriers and grinding the mixture in a suitable mill.
  • Suspension concentrates a) b) c) d) active ingredient mixture 3% 10% 25% 50% ethylene glycol 5% 5% 5% nonylphenol polyglycol ether - 1 % 2% -
  • the finely ground active ingredient is intimately mixed with the adjuvants, yielding a suspension concentrate from which suspensions of any desired concentration can be prepared by dilution with water. It is often more practical for the active ingredients present in the compositions according to the invention to be formulated separately and then to be combined in the applicator in the desired mixing ratio in the form of a "tank mixture", optionally with a diluent such as water, shortly before application.
  • the active ingredients present in the compositions according to the present invention are formulated together (known as pre-mix or formulated product).
  • test compounds exhibit good results.
  • the field tests are carried out in water-saturated ground standing under about 5 cm of water (saturated conditions).
  • the herbicides both on their own and in admixture, are applied to the test plants under water-saturated ground conditions using a back spray.
  • the rates of application depend on the optimum concentrations ascertained under field conditions.
  • Y percentage herbicidal action on treatment with a compound (B) at a rate of application of q kg per hectare, compared with the untreated control.
  • Table B1 Post-emergence herbicidal action of the composition according to the invention comprising prosulfocarb and S-metolachlor at 10 days after application (10 DAA):
  • Table B2 Post-emergence herbicidal action of the composition according to the invention comprising prosulfocarb and S-metolachlor at 10 days after application (10 DAA):
  • Table B3 Post-emergence herbicidal action of the composition according to the invention comprising prosulfocarb and S-metolachlor at 22 days after application (22 DAA):
  • Table B4 Post-emergence herbicidal action of the composition according to the invention comprising prosulfocarb and S-metolachlor at 22 days after application (22 DAA):
  • Table B5 Post-emergence herbicidal action of the composition according to the invention comprising prosulfocarb and S-metolachlor at 22 days after application (22 DAAV
  • Table B6 Post-emergence herbicidal action of the composition according to the invention comprising prosulfocarb and S-metolachlor at 22 days after application (22 DAA):
  • Table B7 Post-emergence herbicidal action of the composition according to the invention comprising prosulfocarb and S-metolachlor at 22 days after application (22 DAA):
  • Table B8 Post-emergence herbicidal action of the composition according to the invention comprising prosulfocarb and fentrazamide at 10 days after application (10 DAA):
  • Table B10 Post-emergence herbicidal action of the composition according to the invention comprising prosulfocarb and fentrazamide at 10 days after application (10 DAA):
  • Table B11 Post-emergence herbicidal action of the composition according to the invention comprising prosulfocarb and fentrazamide at 10 days after application (10 DAA):
  • Table B12 Post-emergence herbicidal action of the composition according to the invention comprising prosulfocarb and fentrazamide at 10 days after application (10 DAA):
  • Table B13 Post-emergence herbicidal action of the composition according to the invention comprising prosulfocarb and fentrazamide at 10 days after application H O DAA):
  • Table B14 Post-emergence herbicidal action of the composition according to the invention comprising prosulfocarb and fentrazamide at 22 days after application (22 DAA):
  • Table B15 Post-emergence herbicidal action of the composition according to the invention comprising prosulfocarb and fentrazamide at 22 days after application (22 DAA):
  • Table B16 Post-emergence herbicidal action of the composition according to the invention comprising prosulfocarb and fentrazamide at 22 days after application (22 DAA):
  • Table B17 Post-emergence herbicidal action of the composition according to the invention comprising prosulfocarb and fentrazamide at 22 days after application (22 DAAV
  • Table B18 Post-emergence herbicidal action of the composition according to the invention comprising prosulfocarb and fentrazamide at 22 days after application (22 DAA):
  • Table B19 Post-emergence herbicidal action of the composition according to the invention comprising prosulfocarb and fentrazamide at 22 days after application (22 DAA):
  • Table B20 Post-emergence herbicidal action of the composition according to the invention comprising prosulfocarb and fentrazamide at 22 days after application (22 DAA):
  • Table B21 Post-emergence herbicidal action of the composition according to the invention comprising prosulfocarb and mefenacet at 10 days after application (10 DAA):
  • Table B22 Post-emergence herbicidal action of the composition according to the invention comprising prosulfocarb and mefenacet at 10 days after application (10 DAA):
  • Table B23 Post-emergence herbicidal action of the composition according to the invention comprising prosulfocarb and mefenacet at 10 days after application (10 DAA):
  • Table B24 Post-emergence herbicidal action of the composition according to the invention comprising prosulfocarb and mefenacet at 10 days after application (10 DAA):
  • Table B25 Post-emergence herbicidal action of the composition according to the invention comprising prosulfocarb and mefenacet at 10 days after application (10 DAA):
  • Table B26 Post-emergence herbicidal action of the composition according to the invention comprising prosulfocarb and mefenacet at 10 days after application (10 DAA):
  • Table B27 Post-emergence herbicidal action of the composition according to the invention comprising prosulfocarb and mefenacet at 22 days after application (22 DAAV
  • Table B28 Post-emergence herbicidal action of the composition according to the invention comprising prosulfocarb and mefenacet at 22 days after application (22 DAA):
  • Table B29 Post-emergence herbicidal action of the composition according to the invention comprisinq prosulfocarb and mefenacet at 22 days after application (22 DAA):
  • Table B30 Post-emergence herbicidal action of the composition according to the invention comprising prosulfocarb and mefenacet at 22 days after application (22 DAA):
  • Table B31 Post-emergence herbicidal action of the composition according to the invention comprisinq prosulfocarb and mefenacet at 22 days after application (22 DAA):
  • Table B32 Post-emergence herbicidal action of the composition according to the invention comprising prosulfocarb and mefenacet at 22 davs after application (22 DAA):
  • Table B33 Post-emergence herbicidal action of the composition according to the invention comprising prosulfocarb and mefenacet at 22 davs after application (22 DAA):
  • Table B34 Post-emergence herbicidal action of the composition according to the invention comprising prosulfocarb and mefenacet at 22 davs after application (22 DAA):
  • Table B35 Post-emergence herbicidal action of the composition according to the invention comprising prosulfocarb and cafenstrole at 10 days after application (10 DAA):
  • Table B36 Post-emergence herbicidal action of the composition according to the invention comprising prosulfocarb and cafenstrole at 10 days after application (10 DAA):
  • Table B37 Post-emergence herbicidal action of the composition according to the invention comprising prosulfocarb and cafenstrole at 10 days after application (10 DAA):
  • Table B38 Post-emergence herbicidal action of the composition according to the invention comprising prosulfocarb and cafenstrole at 22 days after application (22 DAA):
  • Table B39 Post-emergence herbicidal action of the composition according to the invention comprising prosulfocarb and cafenstrole at 22 days after application (22 DAA):
  • Table B40 Post-emergence herbicidal action of the composition according to the invention comprising prosulfocarb and cafenstrole at 22 days after application (22 DAA):
  • Table B41 Post-emergence herbicidal action of the composition according to the invention comprising prosulfocarb and cafenstrole at 22 days after application (22 DAAV
  • Table B42 Post-emergence herbicidal action of the composition according to the invention comprising prosulfocarb and cafenstrole at 22 days after application (22 DAA):

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  • Life Sciences & Earth Sciences (AREA)
  • Agronomy & Crop Science (AREA)
  • Pest Control & Pesticides (AREA)
  • Plant Pathology (AREA)
  • Health & Medical Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Dentistry (AREA)
  • General Health & Medical Sciences (AREA)
  • Wood Science & Technology (AREA)
  • Zoology (AREA)
  • Environmental Sciences (AREA)
  • Agricultural Chemicals And Associated Chemicals (AREA)

Abstract

La présente invention a trait à une composition herbicide comportant une combinaison de principes actifs herbicides de prosulfocarbe et au moins un autre herbicide choisi parmi le naproanilide, napropamide, diphénamide, butachlore, acétochlore, diméthénamide, diméthachlore, alachlore, métolachlore, S-métolachlore, propisochlore, péthoxamide, métazachlore, thénylchlore, propachlore, fentrazamide, flufénacet, méfénacet, anilofos, piperophos et cafenstrole. Chaque combinaison est appropriée pour le contrôle sélectif de végétation indésirable telle que des mauvaises herbes (herbes et mauvaises herbes à larges feuilles) dans des cultures de plantes utiles, par exemple dans des cultures de riz de céréales et de maïs.
EP05824391A 2004-12-17 2005-12-15 Composition herbicide Active EP1827105B1 (fr)

Priority Applications (3)

Application Number Priority Date Filing Date Title
EP05824391A EP1827105B1 (fr) 2004-12-17 2005-12-15 Composition herbicide
PL05824391T PL1827105T3 (pl) 2004-12-17 2005-12-15 Kompozycja herbicydowa
EP08022183A EP2039249A3 (fr) 2004-12-17 2005-12-15 Composition herbicide

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
EP04029973 2004-12-17
EP05824391A EP1827105B1 (fr) 2004-12-17 2005-12-15 Composition herbicide
PCT/EP2005/013510 WO2006063835A2 (fr) 2004-12-17 2005-12-15 Composition herbicide

Related Child Applications (1)

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EP08022183A Division EP2039249A3 (fr) 2004-12-17 2005-12-15 Composition herbicide

Publications (2)

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EP1827105A2 true EP1827105A2 (fr) 2007-09-05
EP1827105B1 EP1827105B1 (fr) 2009-02-25

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EP08022183A Withdrawn EP2039249A3 (fr) 2004-12-17 2005-12-15 Composition herbicide
EP05824391A Active EP1827105B1 (fr) 2004-12-17 2005-12-15 Composition herbicide

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EP08022183A Withdrawn EP2039249A3 (fr) 2004-12-17 2005-12-15 Composition herbicide

Country Status (17)

Country Link
EP (2) EP2039249A3 (fr)
JP (1) JP5053861B2 (fr)
KR (1) KR101317659B1 (fr)
CN (1) CN101080172B (fr)
AR (1) AR052050A1 (fr)
AT (1) ATE423466T1 (fr)
AU (1) AU2005315777B2 (fr)
DE (1) DE602005012986D1 (fr)
EA (2) EA200901394A1 (fr)
ES (1) ES2320790T3 (fr)
GT (1) GT200500371A (fr)
MY (1) MY158017A (fr)
NZ (1) NZ555746A (fr)
PL (1) PL1827105T3 (fr)
TW (1) TWI383749B (fr)
UA (1) UA89210C2 (fr)
WO (1) WO2006063835A2 (fr)

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WO2011082964A1 (fr) * 2009-12-17 2011-07-14 Bayer Cropscience Ag Produits herbicides contenant du flufénacet
WO2011082956A2 (fr) * 2009-12-17 2011-07-14 Bayer Cropscience Ag Agents herbicides contenant du flufénacet
WO2011082955A2 (fr) * 2009-12-17 2011-07-14 Bayer Cropscience Ag Agents herbicides contenant du flufénacet
WO2012029446A1 (fr) 2010-09-01 2012-03-08 株式会社エス・ディー・エス バイオテック Inhibiteur de croissance des bourgeons axillaires du tabac et procédé d'inhibition correspondant
CN104604917B (zh) * 2013-11-04 2016-05-04 南京华洲药业有限公司 一种含麦草畏与唑草胺的除草组合物及其应用
CN105851028A (zh) * 2016-05-20 2016-08-17 潍坊中农联合化工有限公司 苄草丹与高效二甲噻草胺复配除草剂
CN110367270A (zh) * 2019-07-10 2019-10-25 山东省联合农药工业有限公司 一种含苄草丹、吡氟酰草胺和氟噻草胺的除草组合物及其应用
EP4205547A3 (fr) * 2021-12-29 2023-10-11 UPL Corporation Limited Combinaisons herbicides
EP4295684A1 (fr) * 2022-06-22 2023-12-27 Adama Agan Ltd. Composition herbicide agrochimique
EP4295686A1 (fr) * 2022-06-22 2023-12-27 Adama Agan Ltd. Composition herbicide agrochimique
CN116569928A (zh) * 2023-03-09 2023-08-11 上海市农业科学院 一种防除抗性杂草的除草组合物及其应用
CN116806835A (zh) * 2023-06-28 2023-09-29 上海市农业科学院 一种防除抗性杂草的除草组合物及其应用

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Also Published As

Publication number Publication date
PL1827105T3 (pl) 2009-08-31
AU2005315777A1 (en) 2006-06-22
EP2039249A3 (fr) 2009-07-01
GT200500371A (es) 2006-10-25
EP1827105B1 (fr) 2009-02-25
JP2008524148A (ja) 2008-07-10
UA89210C2 (ru) 2010-01-11
EA200701220A1 (ru) 2007-12-28
ATE423466T1 (de) 2009-03-15
JP5053861B2 (ja) 2012-10-24
DE602005012986D1 (de) 2009-04-09
ES2320790T3 (es) 2009-05-28
NZ555746A (en) 2010-04-30
TW200637492A (en) 2006-11-01
CN101080172A (zh) 2007-11-28
TWI383749B (zh) 2013-02-01
AR052050A1 (es) 2007-02-28
MY158017A (en) 2016-08-30
WO2006063835A2 (fr) 2006-06-22
EA013077B1 (ru) 2010-02-26
CN101080172B (zh) 2010-05-12
KR20070089806A (ko) 2007-09-03
KR101317659B1 (ko) 2013-10-15
WO2006063835A3 (fr) 2006-08-03
AU2005315777B2 (en) 2011-03-31
EA200901394A1 (ru) 2010-06-30
EP2039249A2 (fr) 2009-03-25

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